Publikationen von Klaus-Armin Nave
Alle Typen
Zeitschriftenartikel (354)
281.
Zeitschriftenartikel
190 (1), S. 213 - 223 (2004)
Early abnormalities in sciatic nerve function and structure in a rat model of Charcot-Marie-Tooth type 1A disease. Experimental Neurology 282.
Zeitschriftenartikel
40 (3), S. 171 - 175 (2004)
Sox10-rtTA mouse line for tetracycline-inducible expression of transgenes in neural crest cells and oligodendrocytes. Genesis 283.
Zeitschriftenartikel
24 (17), S. 7636 - 7642 (2004)
Cell depletion due to diphtheria toxin fragment A after Cre-mediated recombination. Molecular and Cellular Biology 284.
Zeitschriftenartikel
166 (1), S. 121 - 131 (2004)
Oligodendroglial modulation of fast axonal transport in a mouse model of hereditary spastic paraplegia. Journal of Cell Biology 285.
Zeitschriftenartikel
304 (5671), S. 700 - 703 (2004)
Axonal Neuregulin-1 Regulates Myelin Sheath Thickness. Science 286.
Zeitschriftenartikel
9 (12), S. 1533 - 1537 (2003)
Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A). Nature Medicine 287.
Zeitschriftenartikel
40 (3), S. 501 - 514 (2003)
FAK deficiency in cells contributing to the basal lamina results in cortical abnormalities resembling congenital muscular dystrophies. Neuron 288.
Zeitschriftenartikel
23 (14), S. 6005 - 6012 (2003)
Hippocampal cGMP-dependent protein kinase I supports an age- and protein synthesis-dependent component of long-term potentiation but is not essential for spatial reference and contextual memory. The Journal of Neuroscience 289.
Zeitschriftenartikel
72 (1), S. 12 - 24 (2003)
Genetic background determines phenotypic severity of the Plp rumpshaker mutation. Journal of Neuroscience Research 290.
Zeitschriftenartikel
71 (6), S. 826 - 834 (2003)
Normal metabolism but different physical properties of myelin from mice deficient in proteolipid protein. Journal of Neuroscience Research 291.
Zeitschriftenartikel
33 (3), S. 366 - 374 (2003)
Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination. Nature Genetics 292.
Zeitschriftenartikel
278 (6), S. 3590 - 3598 (2003)
The proteoglycan NG2 is complexed with α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors by the PDZ glutamate receptor interaction protein (GRIP) in glial progenitor cells - Implications for glial-neuronal signaling. The Journal of Biological Chemistry 293.
Zeitschriftenartikel
71 (3), S. 326 - 337 (2003)
Differential expression of L- and S-MAG upon cAMP stimulated differentiation in oligodendroglial cells. Journal of Neuroscience Research 294.
Zeitschriftenartikel
12 (15), S. 1881 - 1895 (2003)
Inactivation of ether lipid biosynthesis causes male infertility, defects in eye development and optic nerve hypoplasia in mice. Human Molecular Genetics 295.
Zeitschriftenartikel
23 (1), S. 277 - 286 (2003)
The C264Y missense mutation in the extracellular domain of L1 impairs protein trafficking in vitro and in vivo. The Journal of Neuroscience 296.
Zeitschriftenartikel
39 (3), S. 256 - 267 (2002)
Phenotypic analysis of mice deficient in the major myelin protein MOBP, and evidence for a novel Mobp isoform. Glia 297.
Zeitschriftenartikel
158 (4), S. 719 - 729 (2002)
Survival of, and competition between, oligodendrocytes expressing different alleles of the Plp gene. Journal of Cell Biology 298.
Zeitschriftenartikel
158 (4), S. 709 - 718 (2002)
Notch1 control of oligodendrocyte differentiation in the spinal cord. Journal of Cell Biology 299.
Zeitschriftenartikel
20 (1), S. 93 - 109 (2002)
Identification of the Regulatory Region of the Peripheral Myelin Protein 22 (PMP22) Gene That Directs Temporal and Spatial Expression in Development and Regeneration of Peripheral Nerves. Molecular and Cellular Neuroscience 300.
Zeitschriftenartikel
157 (2), S. 327 - 336 (2002)
Overexpression of the myelin proteolipid protein leads to accumulation of cholesterol and proteolipid protein in endosomes/lysosomes: implications for Pelizaeus-Merzbacher disease. The Journal of Cell Biology: JCB